- 1,5-Cyclooctadiene
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- $100.00 / 1KG
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2025-09-25
- CAS:111-78-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 1,5-Cyclooctadiene
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- $100.00 / 10kgkg
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2025-06-20
- CAS:111-78-4
- Min. Order: 1kgkg
- Purity: 0.99
- Supply Ability: 1000
- COD
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- $6.00 / 1kg
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2024-01-08
- CAS:
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 5000ton
Related articles - 1,5-cyclooctadiene-bioactivity
- 1,5-Cyclooctadiene is the organic compound with the chemical formula C8H12. Generally abbreviated COD, this diene is a useful ....
- Feb 12，2020
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| Product Name: | 1,5-Cyclooctadiene | | Synonyms: | 1,5-CYCLOOCTADIENE;1,5-CYCLOOCTADIENE, REDISTILLED, 99+%;1,5-Cyclooctadiene, stabilized, 97%;CIS,CIS-1,5-CYCLOOCTADIENE , STABILIZED WITH 50-200PPM IRGANOX 1076;1,5-Cyclooctadiene [stabilized with Octadecyl 3-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)propionate];Cyclooctadiene, 1,5-;1,5-Cyclooctanediene;cis,cis-1,5-Cyclooctadiene: 99%, stabilized with 50-200ppm Irganox 1076 | | CAS: | 111-78-4 | | MF: | C8H12 | | MW: | 108.18 | | EINECS: | 203-907-1 | | Product Categories: | Alkenes;Cyclic;Organic Building Blocks | | Mol File: | 111-78-4.mol |  |
| | 1,5-Cyclooctadiene Chemical Properties |
| Melting point | -69 °C (lit.) | | Boiling point | 149-150 °C (lit.) | | density | 0.882 g/mL at 25 °C (lit.) | | vapor pressure | 25.8 mm Hg ( 37.7 °C) | | refractive index | n20/D 1.493 | | Fp | 89 °F | | storage temp. | 2-8°C | | solubility | soluble in Chloroform | | form | Liquid | | color | Clear colorless | | Odor Threshold | 0.00084ppm | | Water Solubility | 780 mg/L (20 ºC) | | BRN | 2036542 | | Stability: | Stable. Flammable. | | InChI | 1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1-,8-7- | | InChIKey | VYXHVRARDIDEHS-QGTKBVGQSA-N | | SMILES | C1CC=CCCC=C1 | | LogP | 3.16 at 20℃ | | CAS DataBase Reference | 111-78-4(CAS DataBase Reference) | | NIST Chemistry Reference | 1,5-Cyclooctadiene(111-78-4) | | EPA Substance Registry System | 1,5-Cyclooctadiene (111-78-4) |
| | 1,5-Cyclooctadiene Usage And Synthesis |
| Chemical Properties | 1,5-Cyclooctadiene is the organic compound with the chemical formula C8H12.It is a colorless liquid with a strong odor. COD has a boiling point of 151°C and a vapor pressure of 6.8mm at 25°C.
| | Uses | 1,5-Cyclooctadiene is generally abbreviated COD, this diene is a useful precursor to other organic compounds and serves as a ligand in organometallic chemistry. 1,5-Cyclooctadiene can be prepared by dimerization of butadiene in the presence of a nickel catalyst, a coproduct being vinylcyclohexene. It is also a chemical intermediate in the production of Nylon.
| | Chemical Properties | colourless liquid | | Uses | Cycloocta-1,5-diene is produced from petroleum distillation
fractions and is used as an intermediate in the plastics
industry, as a synthetic lubricant, and in numerous other
applications. | | Synthesis Reference(s) | Tetrahedron Letters, 24, p. 3913, 1983 DOI: 10.1016/S0040-4039(00)94312-0 | | Synthesis | Fifty mL of THF was added to a 150 mL flask containing (2.53 mmol) saturated methylsilanes.Ni(COD)2 (0.64 mmol) was dissolved in 25 mL of THF in a separate flask. The flasks were cooled to 0C. The flasks were combined through a cannula. The reaction mixture was heated to room temperature. The mixture was stirred for 1 hour. The flask was drained with a pump. The flask was heated to 70C under vacuum to remove the cyclooctadiene and unreacted methicone. Redissolve the residue in toluene. The residue was filtered. Cooling the saturated toluene solution gave the title compound 1,5-cyclooctadiene by evaporation. | | Carcinogenicity | None of the components present
in this material at concentrations of 0.1% are listed by
IARC, NTP, or OSHA as a carcinogen. | | Purification Methods | Purify it by GLC. It has been purified via the AgNO3 salt. This is prepared by shaking with a solution of 50% aqueous AgNO3 w/w several times (e.g. 3 x 50mLand4x50mL) at 70ofor ca 20minutes to get a good separation of layers. The upper layers are combined and further extracted with AgNO3 at 40o (2 x 20 mL). The upper layer (19 mL) of original hydrocarbon mixture gives colourless needles of the AgNO3 complex on cooling. The adduct is recrystallised from MeOH (and cooling to 0o). The hydrocarbon is recovered by steam distilling the salt. The distillate is extracted with Et2O, dried (MgSO4), filtered, evaporated and distilled. [Jones J Chem Soc 312 1954,[Beilstein 5 H 116, 5 IV 403.] |
| | 1,5-Cyclooctadiene Preparation Products And Raw materials |
| Preparation Products | (3S,4R)-4-Acetoxy-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]azetidin-2-one-->Chloro(1,5-cyclooctadiene)iridium(I) dimer-->Dichloro(cycloocta-1,5-diene)ruthenium(II)-->Bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate-->Chloro(1,5-cyclooctadiene)rhodium(I) dimer-->Dichloro(1,5-cyclooctadiene)platinum(II)-->Dichloro(1,5-cyclooctadiene)palladium(II)-->9-Oxabicyclo[6.1.0]nonan-4-one(8CI,9CI)-->1,3,6-Hexanetricarboxylic acid triethyl ester |
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